ChELSI Institute, Department of Chemical and Biological Engineering, University of Sheffield, Mappin Street, UK.
Metab Eng. 2011 Jul;13(4):445-53. doi: 10.1016/j.ymben.2011.01.004. Epub 2011 Jan 27.
Biotechnology is a promising approach for the generation of hydrogen, but is not yet commercially viable. Metabolic engineering is a potential solution, but has largely been limited to native pathway optimisation. To widen opportunities for use of non-native [NiFe] hydrogenases for improved hydrogen production, we introduced a cyanobacterial hydrogen production pathway and associated maturation factors into Escherichia coli. Hydrogen production is observed in vivo in a hydrogenase null host, demonstrating coupling to host electron transfer systems. Hydrogenase activity is also detected in vitro. Hydrogen output is increased when formate production is abolished, showing that the new pathway is distinct from the native formate dependent pathway and supporting the conclusion that it couples cellular NADH and NADPH pools to molecular hydrogen. This work demonstrates non-native hydrogen production in E. coli, showing the wide portability of [NiFe] hydrogenase pathways and the potential for metabolic engineering to improve hydrogen yields.
生物技术是一种很有前途的制氢方法,但尚未商业化。代谢工程是一种潜在的解决方案,但在很大程度上仅限于天然途径的优化。为了拓宽利用非天然 [NiFe] 氢化酶提高产氢量的机会,我们将一种产氢途径和相关成熟因子引入大肠杆菌中。在氢化酶缺失的宿主中观察到体内产氢,证明与宿主电子传递系统偶联。在体外也检测到氢化酶活性。当消除甲酸盐的产生时,氢气产量增加,表明新途径与天然依赖甲酸盐的途径不同,并支持这样的结论,即它将细胞 NADH 和 NADPH 池与分子氢偶联。这项工作证明了大肠杆菌中非天然产氢,展示了 [NiFe] 氢化酶途径的广泛可移植性和代谢工程提高氢气产量的潜力。